Job Description
Description:
Lab – shipping and obtaining
Regulatory – maintaining binders, signature of the PI – collab with Regulatory
See the patients for data collection, questionnaires, vitals, collect data, EDC entry, answer queries, patient follow up as needed
Screening patients
Consenting patients
Patient recruiting
Specimen processing
Scheduling patients
Regulatory support
Protocol review
Protocol knowledge
Enrolling patients
IRB submissions
Inform Consent Forms
Skills:
Clinical Research, clinical trial, crc, clinical data, pre-screening patients, oncology
Experience Level:
Intermediate Level (2 years of experience REQUIRED)
About Actalent:Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We’re supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.